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3-Pyridazinamine, N-phenyl-, also known as N-Phenyl-3-pyridazinamine or 3-(phenylamino)pyridazine, is an organic compound with the chemical formula C11H10N4. It is a derivative of pyridazine, a heterocyclic aromatic compound consisting of a six-membered ring with two nitrogen atoms at positions 1 and 4. The N-phenyl group is attached to the 3-position of the pyridazine ring, which introduces a phenyl ring (a benzene ring with a hydrogen atom replaced by a nitrogen atom) to the molecule. 3-Pyridazinamine, N-phenyl- is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity.

1011-93-4

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1011-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1011-93-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1011-93:
(6*1)+(5*0)+(4*1)+(3*1)+(2*9)+(1*3)=34
34 % 10 = 4
So 1011-93-4 is a valid CAS Registry Number.

1011-93-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylpyridazin-3-amine

1.2 Other means of identification

Product number -
Other names 3-Anilinopyridazin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1011-93-4 SDS

1011-93-4Downstream Products

1011-93-4Relevant academic research and scientific papers

Ligand-free Ullmann-type C-heteroatom couplings under practical conditions

Gueell, Imma,Ribas, Xavi

, p. 3188 - 3195 (2014)

A new practical ligand-free protocol for copper-catalyzed C-heteroatom cross-coupling reactions (Ullmann-type) is described. The use of dimethyl sulfoxide (DMSO) as the solvent overcomes the need to use organic auxiliary ligands; thus, DMSO is revealed as a nontoxic and superior solvent for Ullmann-type coupling reactions. This method allows the arylation of a wide range of amides, alcohols, and amines under practical conditions with bromobenzene and iodobenzene derivatives and will likely find direct application in current organic synthesis. The competitive reactivity among different functional groups is reported and rationalized, and the possibility to achieve selective arylation reactions is demonstrated. Copyright

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